Genetic Test Details
Neuromuscular Channelopathies Panel
Test Information
- Title
-
Neuromuscular Channelopathies Panel
- Category
- Neurogenetics
- Sub Category
-
Neuromuscular Disease
- Gene/Platform/Region List
-
ATP1A2, CACNA1A, CACNA1S, CLCN1, KCNA1, KCNE3, KCNJ2, SCN4A, SLC12A3
- Test type
- Gene Panel
- Samples Accepted
- Blood, DNA
- Indications
- Carrier Cascade Testing, Diagnosis
- Test Methodology
- Sequencing
- Disease/Condition
-
Neuromuscular Channelopathies, myotonia congenita, paramyotonia congenita, hyperkalemic periodic paralysis, hypokalemic periodic paralysis, Andersen-Tawil syndrome, potassium-aggravated myotonia
Last Updated: January 06, 2026